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Its in the Air

That this is no cheat, this transparent green-wash of the sea which is so amorous after me. [Pg.161]

That it is safe to aiiow it to tick my naked body aii over with its tongues... [Pg.161]

The sweil d and convuis d and congested awake to themseives in condition. [Pg.161]

They pass the invigoration of the night and the chemistry of the night, and awake. .. [Pg.161]

O iove, soive aii, fructify aii with the iast chemistry. —Walt Whitman, Leaves of Grass, ca. 1855 [Pg.161]


The filtrates from the decomposition of the brucine salts with dilute hydrochloride acid should be carefully preserved. The brucine Is recovered by the addition of an excess of dilute ammonia solution (1 4) if the solution becomes turbid before all the ammonia solution is added, introduce a little alcohol until the solution becomes clear. After several hours in an open beaker, filter oft the brucine, wash it well with cold water and dry it in the air. [Pg.507]

Into a 1-litre beaker, provided with a mechanical stirrer, place 36 - 8 g. (36 ml.) of aniline, 50 g. of sodium bicarbonate and 350 ml. of water cool to 12-15° by the addition of a little crushed ice. Stir the mixture, and introduce 85 g. of powdered, resublimed iodine in portions of 5-6 g, at intervals of 2-3 minutes so that all the iodine is added during 30 minutes. Continue stirring for 20-30 minutes, by which time the colour of the free iodine in the solution has practically disappeared and the reaction is complete. Filter the crude p-iodoaniline with suction on a Buchner funnel, drain as completely as possible, and dry it in the air. Save the filtrate for the recovery of the iodine (1). Place the crude product in a 750 ml. round-bottomed flask fitted with a reflux double surface condenser add 325 ml. of light petroleum, b.p. 60-80°, and heat in a water bath maintained at 75-80°. Shake the flask frequently and after about 15 minutes, slowly decant the clear hot solution into a beaker set in a freezing mixture of ice and salt, and stir constantly. The p-iodoaniline crystallises almost immediately in almost colourless needles filter and dry the crystals in the air. Return the filtrate to the flask for use in a second extraction as before (2). The yield of p-iodoaniline, m.p. 62-63°, is 60 g. [Pg.647]

In order to obtain Pt nanoparticles, aqueous solution of 10 M K2PtCl4, which contained 10 M (as monomer unit) of poly-NIPA or poly-NEA, was bubbled with Ar gas and then H2 gas. Then the reaction vessel was sealed tightly and kept in a water bath at a suitable temperature. At given reaction times, the vessels were opened and the samples for transmission electron microscopy (TEM) were prepared by soaking a grid (carbon substrate, Oken) in the colloidal solution and then drying it in the air. The TEM (Hitachi H-8100) was operated at 200 kV. [Pg.301]

DNB can enter your bloodstream if you breathe it in the air or get it on your skin. There is no information on how 1,3,5-TNB can enter or exit your body. Exposure of the general population to... [Pg.15]

Since thorium is found almost everywhere, you will be exposed to small amounts of it in the air you breathe and in the food and water you eat and drink. Scientists know, roughly, the average amounts of thorium in food and drinking water. Most people in the United States eat some thorium with their food every day. Normally, very little of the thorium in lakes, rivers, and oceans gets into the fish or seafood we eat. The amounts in the air are usually so small that they can be ignored. [Pg.11]

Transmission electron microscope ( ) images of such n-Al powders indicate the presence of a thin passivation layer of aluminum oxide (A1203) which provides stability to it in the air. Without this layer, A1 nanoparticles would be pyrophoric and also have tendency to agglomerate to form bulk A1 metal. In order to protect this n-Al powder further, some researchers have suggested its coating with self-assembled nanolayers using perfluoroalkyl carboxylic acid [90]. [Pg.395]

Pour 5 ml of a saturated potassium iodide solution into a test tube. Pass a stream of chlorine through the solution. What substance evolves Filter the substance on a smooth filter and dry it in the air. What impurity will the iodine contain How can it be purified ... [Pg.95]

Check the tightness of the apparatus and fill it with oxygen. Put a small amount of sulphur into a boat, ignite it in the air, and put it into tube 6. Regulate the oxygen stream from the gas meter so... [Pg.123]

Transfer a part of the substance from the boat into a beaker, and pour in two or three drops of a concentrated alkali solution. What gas evolves Put a small amount of the product on a watch glass and leave it in the air. The odour of what gas can be detected What happens to the magnesium nitride in the air ... [Pg.138]

Preparation of Silicon Tetrachloride. To prepare amorphous silicon, mix 2 g of dry quartz sand comminuted in an iron mortar with 3 g of powdered magnesium. Spill the mixture into a refractory test tube, secure it at an angle in a stand, and carefully heat first the entire tube, and then its bottom end more intensively until the mixture ignites. When the reaction ends, break the test tube, extract the product, crush it, and wash it in a fume cupboard, wear eye protection. ) with dilute hydrochloric acid until the flashes of light vanish. Filter off the silicon, wash it on the filter with distilled water, and dry it in the air. [Pg.174]

Grip a small magnesium ribbon (1-2 cm long) with crucible tongs and burn it in the air over a porcelain bowl. Add a few drops of a concentrated alkali solution to the substance obtained and smell the evolving gas. With what components of the air does magnesium react ... [Pg.190]

Reaction of Aluminium with Oxygen and Water. (The experiment is prepared by one student who demonstrates it to the class.) Clean two aluminium plates from aluminium oxide with emery paper and next from grease by boiling them in a small amount of ethanol. Put the plates into a porcelain bowl in a tray with high sides and pour a few drops of a mercury(II) nitrate solution onto them. After five minutes, wash the plates with water, put one of them on a watch glass, and leave it in the air. Immerse the other one into a beaker with water. Observe what occurs and explain these phenomena. Write the equations of the reactions. [Pg.201]

Calculate the amount of ammonium fluoride needed to convert the zirconium tetrafluoride to ammonium heptafluozirconate, and weigh a three-fold excess of the substance (why should the excess ammonium fluoride be taken ). Dissolve the ammonium fluoride in a minimum amount of water (see Appendix 1, Table 1), filter the solution, and add it to the zirconium tetrafluoride solution. If no ammonium heptafluozirconate precipitate appears, add 10-20 ml of ethanol. Filter ofi the precipitate with the aid of a Buchner funnel, rinse it several times on the filter with ethanol, and dry it in the air. [Pg.210]

Using this water, dissolve several crystals of Mohr s salt (what is its composition ) in a test tube, acidify the solution with sulphuric acid, and put a few pieces of iron into it (for what purpose ). Prepare a sodium hydroxide solution in another test tube. By adding the alkali solution to that of the Mohr s salt, prepare a precipitate of iron(II) hydroxide. What is its colour What happens to it in the air Write the equations of the reactions. [Pg.241]

Oxides. Silver(I) Oxide. Introduce 1 ml of a 0.1 N silver nitrate solution into a test tube, and add 1 ml of a 0.1 N sodium hydroxide solution. Wash the precipitate with water by decantation and dry it in the air. What is the composition of the compound ... [Pg.254]

Filter off the substance obtained in the beaker, wash it with water, ethanol, and ether, dry it in the air, and place small portions of it into several test tubes. [Pg.257]

After an hour, extract the unreacted zinc. Filter off the separated metal through a paper filter, wash it with hot water, and dry it in the air. [Pg.263]

As soon as the current is turned on, lead chromate begins to roll off the anode and fall to the bottom of the cell. Very little adheres to the anode plate. After about 2 hr., shut off the current and allow the suspended particles to settle. Decant the clear liquid, wash the precipitate with hot water by a second decantation, collect the solid on a filter, and dry it in the air oven. The yield should be very nearly quantitative for the current used. [Pg.55]

Cognate preparations. p-Nitrobenzaldehyde. This preparation is an example of the Sommelet reaction in which the hexaminium salt is isolated. Dissolve llg (0.13mol) of hexamethylenetetramine in 70ml of chloroform (CAUTION) and add 11.4 g (0.067 mol) of p-nitrobenzyl chloride or 14.4 g of p-nitrobenzyl bromide (Expt 6.28). Heat the mixture under reflux on a steam bath for 4 hours a precipitate gradually separates. Replace the reflux condenser by a condenser set for distillation and distil off about 35 ml of solvent. Add 35 ml of acetone, cool in ice, collect the precipitate by suction filtration and dry it in the air. Heat the hexaminium salt thus obtained under reflux for 1 hour with 100 ml of 50 per cent acetic acid then add 100 ml of water and 25 ml of concentrated hydrochloric acid and continue the refluxing for 5-10 minutes. Cool the solution in ice, collect the crystals of p-nitrobenzaldehyde and dry them in a vacuum desiccator. The yield is 6.4 g (63%), m.p. 106 °C. The p.m.r. spectrum is noted in Expt 6.117. [Pg.1003]

Fmoc-deprotection After the reaction is complete, wash the membrane three times with DMF for at least 30 s each. For storage, wash the modified membrane at least twice with methanol or ethanol and dry it in the air stream of a fume hood or using a hair dryer without heat. For resumption of synthesis after storage, treat the membrane once with DMF for 20 min (see Note 5). The Fmoc-deprotection is carried out by treatment of the membrane twice with 20% piperidine in DMF for at least 5 min each. [Pg.53]

Tetryl can enter your body if you breathe it in the air, drink it in water, or get it on your skin. We do not know the extent to which tetryl enters your body by these routes. Based on limited information from animal studies, tetryl probably leaves your body in urine after being broken down to other substances. See Chapter 2 for more information on how tetryl enters and leaves your body. [Pg.14]


See other pages where Its in the Air is mentioned: [Pg.432]    [Pg.541]    [Pg.700]    [Pg.7]    [Pg.15]    [Pg.432]    [Pg.541]    [Pg.700]    [Pg.111]    [Pg.203]    [Pg.223]    [Pg.432]    [Pg.541]    [Pg.700]    [Pg.869]    [Pg.910]    [Pg.154]    [Pg.869]    [Pg.910]    [Pg.107]    [Pg.109]    [Pg.59]    [Pg.29]   


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